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首页> 外文期刊>Journal of Thoracic Disease >Primary mediastinal leiomyoma: a rare case report and literature review
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Primary mediastinal leiomyoma: a rare case report and literature review

机译:原发性纵隔平滑肌瘤:一例罕见病例报告并文献复习

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Primary mediastinal leiomyomas are extremely rare, its etiology unknown, and up to the present has only been described in a few cases in the English literature. In this case report, we describe a 3-year-old girl with asymptomatic left upper quadrant abdominal mass. Chest computed tomography demonstrated a giant solid mass in the anterior mediastinum, which extended to the right hemi-thorax and left upper quadrant abdomen. Fortunately, the girl underwent a complete surgical tumor resection. The definitive diagnosis was primary mediastinal leiomyoma. To our best knowledge, this is the second case report of primary mediastinal leiomyoma of child.
机译:原发性纵隔平滑肌瘤极为罕见,其病因尚不明确,到目前为止,仅在英国文献中有少数病例进行过描述。在此病例报告中,我们描述了一个无症状的左上腹腹部肿块的3岁女孩。胸部计算机断层扫描显示前纵隔有巨大的实性肿块,延伸至右半胸和左上腹腹部。幸运的是,这名女孩接受了一次完整的手术肿瘤切除术。明确的诊断是原发性纵隔平滑肌瘤。据我们所知,这是儿童原发性纵隔平滑肌瘤的第二例病例报告。

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